Canonical Allele Identifier: CA2996383224

Gene: NFKBIA

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35404618_35404619insAGGCGGCCGAGCGCCCCCAGGAG , CM000676.2:g.35404618_35404619insAGGCGGCCGAGCGCCCCCAGGAG	GRCh38
NC_000014.8:g.35873824_35873825insAGGCGGCCGAGCGCCCCCAGGAG , CM000676.1:g.35873824_35873825insAGGCGGCCGAGCGCCCCCAGGAG	GRCh37
NC_000014.7:g.34943575_34943576insAGGCGGCCGAGCGCCCCCAGGAG	NCBI36
NG_007571.1:g.5120_5121insCTCCTGGGGGCGCTCGGCCGCCT , LRG_89:g.5120_5121insCTCCTGGGGGCGCTCGGCCGCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553342.2:c.26_27insCTCCTGGGGGCGCTCGGCCGCCT	ENSP00000451281.2:p.Gln9HisfsTer20
ENST00000557459.2:n.124_125insCTCCTGGGGGCGCTCGGCCGCCT
ENST00000697957.1:n.131_132insCTCCTGGGGGCGCTCGGCCGCCT
ENST00000697958.1:n.124_125insCTCCTGGGGGCGCTCGGCCGCCT
ENST00000697959.1:n.131_132insCTCCTGGGGGCGCTCGGCCGCCT
ENST00000697960.1:n.111_112insCTCCTGGGGGCGCTCGGCCGCCT
ENST00000697961.1:c.26_27insCTCCTGGGGGCGCTCGGCCGCCT	ENSP00000513487.1:p.Gln9HisfsTer20
ENST00000697966.1:n.49-5_49-4insCTCCTGGGGGCGCTCGGCCGCCT
ENST00000216797.10:c.26_27insCTCCTGGGGGCGCTCGGCCGCCT MANE Select	ENSP00000216797.6:p.Gln9HisfsTer20
ENST00000216797.9:c.26_27insCTCCTGGGGGCGCTCGGCCGCCT	ENSP00000216797.5:p.Gln9HisfsTer20
ENST00000553342.1:c.26_27insCTCCTGGGGGCGCTCGGCCGCCT	ENSP00000451281.1:p.Gln9HisfsTer20
ENST00000554001.5:c.26_27insCTCCTGGGGGCGCTCGGCCGCCT	ENSP00000450537.1:p.Gln9HisfsTer20
ENST00000555629.1:n.131_132insCTCCTGGGGGCGCTCGGCCGCCT
ENST00000557100.5:n.82_83insCTCCTGGGGGCGCTCGGCCGCCT
ENST00000557140.5:c.26_27insCTCCTGGGGGCGCTCGGCCGCCT	ENSP00000451257.1:p.Gln9HisfsTer20
ENST00000557459.1:n.124_125insCTCCTGGGGGCGCTCGGCCGCCT
NM_020529.2:c.26_27insCTCCTGGGGGCGCTCGGCCGCCT , LRG_89t1:c.26_27insCTCCTGGGGGCGCTCGGCCGCCT	NP_065390.1:p.Gln9HisfsTer20
NM_020529.3:c.26_27insCTCCTGGGGGCGCTCGGCCGCCT MANE Select	NP_065390.1:p.Gln9HisfsTer20